Linked Data
dbSNP Id:
rs2097504149
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122508487T>G , CM000672.2:g.122508487T>G | GRCh38 |
| NC_000010.10:g.124268003T>G , CM000672.1:g.124268003T>G | GRCh37 |
| NC_000010.9:g.124257993T>G | NCBI36 |
| NG_011554.1:g.51963T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.1006-169T>G MANE Select | ENSP00000357980.3:n.1006-169T>G | |
| ENST00000648167.1:c.688-169T>G | ENSP00000498033.1:n.688-169T>G | |
| ENST00000368984.7:c.1006-169T>G | ENSP00000357980.3:n.1006-169T>G | |
| ENST00000420892.1:c.229-169T>G | ENSP00000412676.1:n.229-169T>G | |
| NM_002775.4:c.1006-169T>G | NP_002766.1:n.1006-169T>G | |
| NM_002775.5:c.1006-169T>G MANE Select | NP_002766.1:n.1006-169T>G |